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Insertion/Deletion Polymorphism and Other Restriction Fragment Length Polymorphisms in the MCC Gene

The MCC gene is a candidate as a tumor suppressor gene for colorectal neoplasms. Further, MCC is tightly linked to the familial adenomatous polyposis (FAP) locus by linkage and physical analysis. Hence, restriction fragment length polymorphisms (RFLPs) of this gene might be very useful for presympto...

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Autores principales: Miyoshi, Yasuo, Nishisho, Isamu, Miki, Yoshio, Mori, Takesada, Kinzler, Kenneth W., Vogelstein, Bert, Nakamura, Yusuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1992
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918660/
https://www.ncbi.nlm.nih.gov/pubmed/1347524
http://dx.doi.org/10.1111/j.1349-7006.1992.tb02344.x
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author Miyoshi, Yasuo
Nishisho, Isamu
Miki, Yoshio
Mori, Takesada
Kinzler, Kenneth W.
Vogelstein, Bert
Nakamura, Yusuke
author_facet Miyoshi, Yasuo
Nishisho, Isamu
Miki, Yoshio
Mori, Takesada
Kinzler, Kenneth W.
Vogelstein, Bert
Nakamura, Yusuke
author_sort Miyoshi, Yasuo
collection PubMed
description The MCC gene is a candidate as a tumor suppressor gene for colorectal neoplasms. Further, MCC is tightly linked to the familial adenomatous polyposis (FAP) locus by linkage and physical analysis. Hence, restriction fragment length polymorphisms (RFLPs) of this gene might be very useful for presymptomatic diagnosis of individuals in families segregating mutant alleles of the APC gene. Here we report the identification of five polymorphic systems in MCC gene (both cDNA and genomic), one of which is an insertion/deletion polymorphism that is detectable by a polymerase chain reaction method. These five RFLP systems should be useful for linkage studies in FAP and for examining loss of heterozygosity at this locus in colonic polyps and tumors.
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spelling pubmed-59186602018-05-11 Insertion/Deletion Polymorphism and Other Restriction Fragment Length Polymorphisms in the MCC Gene Miyoshi, Yasuo Nishisho, Isamu Miki, Yoshio Mori, Takesada Kinzler, Kenneth W. Vogelstein, Bert Nakamura, Yusuke Jpn J Cancer Res Rapid Communication The MCC gene is a candidate as a tumor suppressor gene for colorectal neoplasms. Further, MCC is tightly linked to the familial adenomatous polyposis (FAP) locus by linkage and physical analysis. Hence, restriction fragment length polymorphisms (RFLPs) of this gene might be very useful for presymptomatic diagnosis of individuals in families segregating mutant alleles of the APC gene. Here we report the identification of five polymorphic systems in MCC gene (both cDNA and genomic), one of which is an insertion/deletion polymorphism that is detectable by a polymerase chain reaction method. These five RFLP systems should be useful for linkage studies in FAP and for examining loss of heterozygosity at this locus in colonic polyps and tumors. Blackwell Publishing Ltd 1992-01 /pmc/articles/PMC5918660/ /pubmed/1347524 http://dx.doi.org/10.1111/j.1349-7006.1992.tb02344.x Text en
spellingShingle Rapid Communication
Miyoshi, Yasuo
Nishisho, Isamu
Miki, Yoshio
Mori, Takesada
Kinzler, Kenneth W.
Vogelstein, Bert
Nakamura, Yusuke
Insertion/Deletion Polymorphism and Other Restriction Fragment Length Polymorphisms in the MCC Gene
title Insertion/Deletion Polymorphism and Other Restriction Fragment Length Polymorphisms in the MCC Gene
title_full Insertion/Deletion Polymorphism and Other Restriction Fragment Length Polymorphisms in the MCC Gene
title_fullStr Insertion/Deletion Polymorphism and Other Restriction Fragment Length Polymorphisms in the MCC Gene
title_full_unstemmed Insertion/Deletion Polymorphism and Other Restriction Fragment Length Polymorphisms in the MCC Gene
title_short Insertion/Deletion Polymorphism and Other Restriction Fragment Length Polymorphisms in the MCC Gene
title_sort insertion/deletion polymorphism and other restriction fragment length polymorphisms in the mcc gene
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918660/
https://www.ncbi.nlm.nih.gov/pubmed/1347524
http://dx.doi.org/10.1111/j.1349-7006.1992.tb02344.x
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